CVS IODINE- iodine, sodium iodide and alcohol liquid

País: Estados Unidos

Idioma: inglés

Fuente: NLM (National Library of Medicine)

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20-12-2023

Ingredientes activos:

IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4), SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q), ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Disponible desde:

CVS Pharmacy

Designación común internacional (DCI):

IODINE

Composición:

IODINE 20 mg in 1 mL

Vía de administración:

TOPICAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

Antiseptic To help prevent infection in minor cuts, scrapes, and burns.

Estado de Autorización:

OTC monograph not final

Ficha técnica

                                CVS IODINE- IODINE, SODIUM IODIDE AND ALCOHOL LIQUID
CVS PHARMACY
----------
CVS IODINE TINCTURE USP
CVS IODINE TINCTURE USP
Drug Facts
ACTIVE INGREDIENT
Iodine 2%
Sodium Iodide 2.4%
Alcohol 47%
PURPOSE
Antiseptic
INDICATIONS
To help prevent infection in minor cuts, scrapes, and burns.
WARNINGS:
FOR EXTERNAL USE ONLY
ASK A DOCTOR BEFORE USE IF YOU HAVE
Deep or puncture wounds
Animal bites
Serious burns
STOP USE AND ASK A DOCTOR IF
the condition persists or gets worse, if using this product for longer
than 1 week.
WHEN USING THIS PRODUCT
DO NOT USE
in the eyes. If contact occurs, flush with large amounts of water
while lifting upper and
lower lids.
DO NOT APPLY
over large areas of the body.
KEEP OUT OF REACH OF CHILDREN.
In case of accidental ingestion. Give milk, then give a starch
solution made by mixing
two tablespoofuls of cornstarch or flour to a pint of water. Contact a
Poison Control
Center immediately.
DIRECTIONS
Clean the affected area; apply a small amount on the area 1 to 3 times
daily; may be
covered with a sterile bandage. If bandaged, let dry first.
INACTIVE INGREDIENT
Purified water.
OTHER INFORMATION
Will stain skin and clothing
PRINCIPAL DISPLAY PANEL
CVS Health
Iodine Tincture USP
First Aid Antiseptic
1 FL OZ (30 mL)
CVS IODINE
iodine, sodium iodide and alcohol liquid
CVS Pharmacy
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:69842-213
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)
IODINE
20 mg in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)
IODIDE ION
20.4 mg in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
470 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:69842-
213-91
30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a
Combination Product
01/01/2008
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION
                                
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